• Methyl CpG Binding Protein 2 (MECP2) Gene Mutation Analysis, Rett Syndrome
  • Cysticercosis Antibody, IgG, CSF
  • Gelsolin (GSN) Gene Mutation Analysis
  • Sphingomyelin Phosphodiesterase 1 (SMPD1) Mutation Analysis, Niemann-Pick Disease
  • Lead/Creatinine Ratio, Random, Urine
  • Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
  • Endomysial (EMA) Antibody, IgG and IgM
  • Imipramine, Urine
  • Metanephrines, Plasma
  • Cytochrome P450 2B6 (CYP2B6) Genotyping
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Long QT Syndrome Multi-Gene Panel, NGS
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Long QT Syndrome Multi-Gene Panel, NGS
Medical Test

Clinical Utility
Access to Long QT Syndrome Multi-Gene Panel, NGS is restricted.